Stryker Howmedica Osteonics Corp.: Medical Device Recall in 2014 - (Recall #: Z-0964-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Stryker Orthopaedics Navigation Compatible Accolade Broach Handle 1 single unit to a package Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430 USA Stryker France ZAC Satolas Green Pusignan Av de Satolas Green 69881 Meyzieu Cedex France Made in USA non-sterile

Product Classification:

Class II

Date Initiated: November 20, 2013

Date Posted: February 19, 2014

Recall Number: Z-0964-2014

Event ID: 67234

Reason for Recall:

Stryker received reports from the field of the impaction plate dissociating/fracturing from the main body of the broach handle.

Status: Terminated

Product Quantity: 211 units

Code Information:

Catalog no. 2124-1400 All lots

Distribution Pattern:

IL MA, MN, ND, OR, & PA

Voluntary or Mandated:

Voluntary: Firm initiated